Description |
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 1 |
cell death inducing DFFA like effector b |
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GO Annotations |
Cellular Component |
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Molecular Function |
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Biological Process |
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Pathways |
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Drugs |
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Diseases |
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GWAS |
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- Anorectal malformation ( 31136621)
- Height ( 28552196)
- Parent of origin effect on language impairment (paternal) ( 24571439)
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Interacting Genes |
54 interacting genes:
ADAMTSL4
ADD1
AKT1
CCNE1
CEBPB
CFP
CIDEB
CYSRT1
EWSR1
FANCA
FUS
GATA1
GLRX3
GSTO2
ITCH
KLF1
KRTAP13-3
KRTAP19-2
KRTAP21-2
KRTAP22-1
KRTAP26-1
KRTAP3-1
KRTAP3-2
KRTAP3-3
KRTAP6-1
KRTAP6-2
KRTAP6-3
KRTAP7-1
LRP2BP
MGAT5B
MSL1
MYC
NCOA1
NEDD4
NONO
NR3C1
OTX1
PLSCR1
PPIP5K2
PRMT5
PTH1R
RELB
SIN3A
SLC15A2
SMARCA4
SMARCD3
SP1
SPATA12
STT3B
TAF15
TRIM42
UFSP1
VGLL3
ZNF581
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68 interacting genes:
ABHD16A
AFG1L
APOC1
ARL8B
ATP5ME
ATP5MJ
BCL2L2
C5orf38
CAND2
CIDEA
CLCN1
CMPK1
COL10A1
COL8A1
COX7C
DFFA
DFFB
DHRSX
DNAJA3
FAM218A
FAM47E-STBD1
FKBP8
FOXD4L3
FUNDC2
GCSH
GNB3
GPAM
H4C7
HAPLN2
HCCS
HIGD1C
MEST
MICOS10
MPC2
MRPL36
MRPL57
MTERF4
NAALAD2
NDRG4
NFU1
NME4
PBX3
PDHX
PGLYRP3
PISD
PPIF
RAMP2
RHBDD2
ROMO1
RTP5
SAA2
SAA4
SAR1B
SCO1
SCO2
SDHAF1
SFXN1
SMARCC1
SPG21
TAOK2
TBX2
TEX44
THBD
TIMM17B
TMEM14B
TPRG1
TSR1
UFSP1
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Entrez ID |
6599 |
27141 |
HPRD ID |
03435 |
11981 |
Ensembl ID |
ENSG00000173473
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ENSG00000136305
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Uniprot IDs |
Q58EY4
Q92922
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Q9UHD4
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PDB IDs |
2YUS
5GJK
6KZ7
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1D4B
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
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Tagcloud (Difference) ? |
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Tagcloud (Intersection) ? |
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